Case 8: Optometry® Color Fundus and AF Comparison OD and OS
KEY:
Color Optomap
Auto Fluorescence
This pattern is typical of pericentral RP, which is usually an autosomal dominant inherIted disorder. Many of these patients have minimal or no symptoms, reveal slow progression when followed carefully over time, and have several known genetic defects. Cases of pericentral RP in 4 consecutive generations have been reported.
